CN101609735A - High-purity high-density high yield Si 3N 4/ SiO 2The preparation method of coaxial nano-cable array - Google Patents

High-purity high-density high yield Si 3N 4/ SiO 2The preparation method of coaxial nano-cable array Download PDF

Info

Publication number
CN101609735A
CN101609735A CNA2009100894592A CN200910089459A CN101609735A CN 101609735 A CN101609735 A CN 101609735A CN A2009100894592 A CNA2009100894592 A CN A2009100894592A CN 200910089459 A CN200910089459 A CN 200910089459A CN 101609735 A CN101609735 A CN 101609735A
Authority
CN
China
Prior art keywords
sio
coaxial nano
cable
nano
substrate
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
CNA2009100894592A
Other languages
Chinese (zh)
Other versions
CN101609735B (en
Inventor
彭志坚
朱娜
王成彪
付志强
于翔
岳�文
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
China University of Geosciences
China University of Geosciences Beijing
Original Assignee
China University of Geosciences Beijing
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by China University of Geosciences Beijing filed Critical China University of Geosciences Beijing
Priority to CN2009100894592A priority Critical patent/CN101609735B/en
Publication of CN101609735A publication Critical patent/CN101609735A/en
Application granted granted Critical
Publication of CN101609735B publication Critical patent/CN101609735B/en
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Images

Landscapes

  • Silicon Compounds (AREA)
  • Catalysts (AREA)

Abstract

The present invention relates to the Si of a kind of high-purity, high density, high yield 3N 4/ SiO 2The preparation method of coaxial nano-cable array belongs to technical field of material.The present invention adopts the pyrolysis organic precursor being coated with synthetic Si on the substrate of metallic catalyst 3N 4/ SiO 2Coaxial nano-cable array.Contain the crosslinked at low temperature curing of polysilazane under 160-300 ℃ of (1) high nitrogen content in steps, obtain translucent amorphous SiCN solid; (2) high-energy ball milling, the pulverizing of amorphous SiCN solid in the high abrasion utensil behind the crosslinking curing; (3) high temperature pyrolysis, the evaporation of the precursor powder that obtains behind the high-energy ball milling under the carrier gas protection that contains a certain amount of oxygen, and deposition obtains described structure on the substrate that is coated with the metal catalytic agent film.Described method synthesis technique and equipment are simple, and the technological parameter controllability is strong, and is with low cost, gained Si 3N 4/ SiO 2The coaxial nano cable growth is orderly, and output is big, density is high, purity is high and diameter is evenly distributed.The coaxial nano cable structure of being synthesized has wide practical use at aspects such as atomic force microscope, NFM, nanometer mechanics probe and novel nano composite material reinforcing agents.

Description

High-purity high-density high yield Si 3N 4/ SiO 2The preparation method of coaxial nano-cable array
Technical field
The present invention relates to a kind of high-purity, high density, high yield Si 3N 4/ SiO 2The preparation method of coaxial nano-cable array belongs to technical field of material.
Background technology
Found that from French scientist Colliex in 1997 etc. C-BN-C is with axial system and since naming it to be coaxial nano cable in the product that arc discharge obtains, coaxial nano cable has caused various countries scientists' very big interest, becomes a focus of nano materials research very soon.The kernel of coaxial nano cable is generally semiconductor or metal nanometer line, and the sheath layer is heterogeneous conductor or insulator shell, and kernel and sheath layer are coaxial.Coaxial nano cable has a wide range of applications at numerous areas with its special core/shell structure and unique light, electricity, magnetic performance, it can be used as the connecting line between the high density integrated component, the parts of ultracapacitor, microtool box and microrobot, also can be used as the needle point of miniature probe, be used for the detection instrument of important nanometer resolution such as atomic force microscope and nanometer mechanics probe.In addition, coaxial nano cable also can be used as the reinforcing agent of composite material, because of its coating can be selected the material that is complementary with matrix, thereby improves performance of composites.And aspect basic research, coaxial nano cable provides condition for the Physical Experiment research of one dimension system, for example, can study under the condition of coating confinement, the electron transport behavior of core nano wire, the motor behavior of phonon and photon, and the essential characteristic of calorifics behavior, therefrom find new phenomenon, new rule, for the new theory of setting up accurate 1-dimention nano system lay the foundation (Zhang Lide. the newcomer of quasi-one-dimensional nanometer material family---coaxial nano cable. Bulletin of Chinese Academy of Sciences, 1999,5:350-352).
The coaxial nano cable of exploring preparation high-purity, high yield and diameter narrowly distributing is the focus that people pay close attention to always.Up to the present, existing a variety of methods are used for preparing the nano-cable with coaxial configuration, as hydro thermal method, sol-gel process, template, vapour deposition process, laser ablation method etc., utilize these methods, the coaxial nano cable of having prepared different types of material is as Ge/SiO x, Zn/ZnO, SiC/SiO 2, Ga-doped Si 3N 4/ SiON, α-Si 3N 4/ Si/SiO 2Deng.
Si 3N 4Material has high strength, high rigidity, good resistance to wear, thermal shock resistance and excellent properties such as anti-oxidant, but also is the semi-conducting material of a kind of broad stopband (5.3eV), Si 3N 4/ SiO 2SiO in the coaxial nano cable 2Shell has good insulating properties, and can prevent oxidation and prevent the radiation damage to nanostructure such as electron beam, thereby Si 3N 4/ SiO 2Coaxial nano cable can be used to prepare high-performance composite materials, and the nano electron device that uses under severe rugged environments such as high temperature and high radiation.At present, bibliographical information only has people (G.Z.Ran, L.P.You, L.Dai, et al.Catalystless synthesis ofcrystalline Si such as G.Z.Ran 3N 4/ amorphous SiO 2Nanocables from silicon substrates and N 2.Chemical PhysicsLetters, 2004,384:94-97) without catalyst synthetic Si that has obtained chaotic on silicon chip 3N 4/ SiO 2Coaxial nano cable, but the distribution of chaotic will cause the application of nano-cable limited, because constructing of nano-device need be assembled in order to monodimension nanometer material, make it have array structure, and realize the design of its performance is regulated and control, this also is the design basis of nanometer superminiature device.Yet there are no relevant Si 3N 4/ SiO 2The bibliographical information of coaxial nano-cable array.
Summary of the invention
The objective of the invention is to propose a kind of Si 3N 4/ SiO 2The preparation method of coaxial nano-cable array.It is unique evaporation source that this method adopts the organic polymer precursor body of high nitrogen, silicone content, by the method for pyrolysis, under the oxygen partial pressure condition in strictness control reaction atmosphere, being coated with on the appointment substrate of catalyst film, prepares Si 3N 4/ SiO 2Coaxial nano-cable array.This method has that the reaction condition strictness is controlled, experimental facilities and technology is simple, product yield is high, advantage such as with low cost, the Si that is obtained 3N 4/ SiO 2Coaxial nano-cable array, kernel are the monocrystalline silicon nitride, and shell is an amorphous silica, product purity height, density height, and along the nanostructure growth direction, the kernel in the nanostructure and the diameter of shell distribute all very even, diameter and length controlled.
The Si that the present invention proposes 3N 4/ SiO 2Coaxial nano-cable array preparation method is characterized in that, described method adopts pyrolysis evaporation organic precursor method being coated with synthetic Si on the substrate of catalyst 3N 4/ SiO 2Coaxial nano-cable array may further comprise the steps:
(1) polysilazane of high nitrogen content under high pure nitrogen, argon gas or ammonia atmosphere, through catalysis or do not have the catalysis heat cross-linking and solidified 0.5-2 hour, obtains translucent SiCN amorphous solid under 160-300 ℃;
(2) should in the agate container, smash to pieces by translucent amorphous solid, mix with the high abrasion zirconium oxide balls then, in the polyurethane ball grinder, on high energy ball mill, ground 2-24 hour, obtain the amorphous state SiCN powder of particle diameter less than 0.2 μ m;
(3) an amount of amorphous state SiCN powder through behind the ball milling is placed on corundum crucible at the bottom of; the substrate that is coated with catalyst is placed the top of powder in the crucible; under the prerequisite that keeps certain oxygen partial pressure; make carrier gas and protection gas with nitrogen or ammonia; be warmed up to design temperature with extremely low speed; be incubated the some time then, can on substrate, obtain the Si of high-purity, high density, high yield 3N 4/ SiO 2Coaxial nano-cable array.
In above-mentioned preparation method, the unique evaporation source in the described step (1) is the polysilazane of high nitrogen content.
In above-mentioned preparation method, the amorphous solid behind the crosslinking curing in the described step (2) in the high abrasion container, under the high abrasion abrading-ball effect under levigate, can not introduce any other surfactant granules.
In above-mentioned preparation method, the amorphous solid behind the crosslinking curing in the described step (2) is after levigate, and particle diameter is less than 0.2 μ m.
In above-mentioned preparation method, the amorphous state SiCN powder in the described step (3) behind institute's crosslinking curing that adopts, quality is that 0.1-5.0 restrains.
In above-mentioned preparation method, the substrate in the described step (3) is a kind of among silicon chip, gallium arsenide film, sapphire sheet, silicon nitride single crystal sheet, quartz plate, the alumina formwork, and surfacing, and fineness is good.
In above-mentioned preparation method, deposited a kind of among layer of even metallic catalyst Fe, Co, Ni, the Cu film on the substrate in the described step (3), and thickness is 2-50nm.
In above-mentioned preparation method, adopt higher nitrogen of purity or ammonia to make carrier gas and protection gas in the described step (3), but wherein oxygen partial pressure is controlled at 10 -19To 10 -5Between the individual standard atmospheric pressure.
In above-mentioned preparation method, the heating rate in the described step (3) is 0.5 ℃/minute to 10 ℃/minute.
In above-mentioned preparation method, the pyrolysis temperature in the described step (3) is 1100 ℃ to 1450 ℃.
In above-mentioned preparation method, the temperature retention time under the maximum temperature in the described step (3) is 15 minutes to 4 hours,
In above-mentioned preparation method, the single crystalline Si in the described step (3) 3N 4The substrate of nano-array growth is from being 0-20mm by the distance of the crosslinking curing powder of pyrolysis.
Adopt present technique to prepare Si 3N 4/ SiO 2Coaxial nano-cable array is compared with the preparation method of traditional coaxial nano cable, and equipment and technology are simple, product yield is high, with low cost, the Si that is obtained 3N 4/ SiO 2Coaxial nano cable growth becomes array, density height in order, and nuclear, shell are even along nanostructure growth direction diameter, length controlled, purity height.
Description of drawings
Fig. 1 is the embodiment of the invention 1 prepared α-Si 3N 4/ SiO 2The x-ray diffraction pattern of coaxial nano-cable array
Fig. 2 is the embodiment of the invention 1 prepared α-Si 3N 4/ SiO 2The ESEM surface picture of coaxial nano-cable array
Fig. 3 is the embodiment of the invention 1 prepared α-Si 3N 4/ SiO 2Coaxial nano-cable array ESEM section photo
Fig. 4 is the embodiment of the invention 1 prepared α-Si 3N 4/ SiO 2The transmission electron microscope photo of the single nanostructure of coaxial nano-cable array
Fig. 5 is the embodiment of the invention 1 prepared α-Si 3N 4/ SiO 2The high-resolution-ration transmission electric-lens photo of the single nanostructure of coaxial nano-cable array
Embodiment
Below in conjunction with embodiment technical scheme of the present invention is described further.
The present invention proposes a kind of Si 3N 4/ SiO 2The preparation method of coaxial nano-cable array is characterized in that, described method adopts the pyrolysis organic precursor being coated with synthetic Si on the substrate of catalyst 3N 4/ SiO 2Coaxial nano-cable array, and comprise the steps and content:
(1) polysilazane that adopts, silicon, nitrogen content height surpass 15at% and 20at% respectively, and oxygen content is no more than 3at%, and is described method deposition Si 3N 4/ SiO 2Unique silicon source of coaxial nano-cable array.
(2) polymer precursor is under high pure nitrogen, argon gas or ammonia atmosphere, through catalysis or do not have the catalysis heat cross-linking and solidified 0.5-2 hour, decomposes and removes moisture and most of hydrogen under 160-300 ℃, becomes translucent SiCN amorphous solid.
(3) this translucent amorphous solid is smashed to pieces in the agate container of high abrasion, mix with the high abrasion zirconium oxide balls then, be contained in the polyurethane ball grinder of high abrasion, on high energy ball mill, ground 2-24 hour, obtain the powder of particle diameter less than 0.2 μ m.Whole process is not introduced surfactant granules substantially, is beneficial to presoma and at high temperature evaporates, and can growth in situ do not obtain the nano material of other structures.
(4) be 2-50nm thick metallic catalyst Fe, Co, Ni or Cu film with magnetron sputtering coater in any surface finish, through deposition one layer thickness on silicon chip, gallium arsenide film, sapphire sheet, silicon nitride single crystal sheet, quartz plate or the alumina formwork of ultrasonic cleaning in advance.
(5) 0.1-5.0 is restrained at the bottom of the precursor powder that ball milling obtains is placed on corundum crucible, the substrate that is coated with catalyst is placed the 0-20mm place, top of powder in the crucible.
(6) adopt higher nitrogen of purity or ammonia to make carrier gas and protection gas, keep constant gas in the whole process, and wherein oxygen partial pressure is controlled at 10 -19To 10 -5Between the individual standard atmospheric pressure.
(7) slowly be heated to 1100-1450 ℃ with 0.5 ℃/minute to 10 ℃/minute heating rate, and be incubated 15 minutes to 4 hours.
Resultant Si 3N 4/ SiO 2Coaxial nano-cable array is white film in appearance.
Under scanning electron microscopy, can observe the nano-structure array of the ordering growth of high yield, and can obviously observe Si in that transmission electron microscope is next 3N 4/ SiO 2The coaxial nano cable structure.
In a word, show comprehensively that this array is countless Si through various analytical tests 3N 4/ SiO 2The coaxial nano cable structure is formed, and wherein, single nanostructure is that monocrystalline α-Dan Huagui, shell are formed for the amorphous silica layer by kernel.
Embodiment 1: initial feed is polysilazane perhydropolysilazane; be light yellow viscous liquid under the room temperature, solidify 0.5h at 260 ℃ of following catalyst-free heat cross-linkings, protective atmosphere is a nitrogen; throughput is 40ml/min, obtains translucent amorphous state SiCN solid.Placing agate mortar to smash to pieces the SiCN solid, is the high abrasion PZT abrading-ball mixing of 2mm with diameter then, in the polyurethane ball grinder, grinds 10 hours on high energy ball mill.Get the precursor powder of 0.3 gram through solidifying, pulverizing, be evenly distributed on the corundum crucible bottom, cutting small pieces then, to be coated with thickness be that the silicon chip of the thick Fe film of 5nm is placed on the high ZrO of the powder about 2mm in top 2On the support.Be placed on then and carry out high temperature pyrolysis in the tube furnace, behind insulation 2h under 1250 ℃, naturally cool to room temperature and make Si 3N 4/ SiO 2Coaxial nano-cable array.Protective atmosphere is commercially available high pure nitrogen, and gas flow rate is 60ml/min.
Can obviously detect the α-Dan Huagui phase in the nano array structure that is synthesized, also detected silicon dioxide amorphous bag (see figure 1) simultaneously, this nanostructure is high yield ordered structure, density very high (seeing Fig. 2 and 3), the external diameter of coaxial nano cable is 60-120nm, internal diameter is 20-90nm, and kernel is the silicon nitride of monocrystalline, and shell is the silicon dioxide layer of amorphous, and growth is (seeing Figure 4 and 5) very evenly, and the high (see figure 4) of purity.

Claims (4)

1. high-purity, high density, high yield Si 3N 4/ SiO 2The preparation method of coaxial nano-cable array is characterized in that: described method is being coated with synthetic Si on the substrate of catalyst by the pyrolysis organic precursor 3N 4/ SiO 2Coaxial nano-cable array may further comprise the steps:
(1) polysilazane of high nitrogen content under high pure nitrogen, argon gas or ammonia atmosphere, through catalysis or do not have the catalysis heat cross-linking and solidified 0.5-2 hour, obtains the amorphous solid of translucent SiCN under 160-300 ℃;
(2) should in the agate container, smash to pieces by translucent SiCN amorphous solid, mix with the high abrasion zirconium oxide balls then, in the polyurethane ball grinder, on high energy ball mill, ground 2-24 hour, obtain particle diameter less than 0.2 μ m amorphous state SiCN powder;
(3) at the bottom of the precursor powder through behind the crosslinking curing of ball milling that 0.1-5.0 is restrained is placed on corundum crucible; the substrate that is coated with catalyst is placed the 2-20mm place, top of powder in the crucible; under nitrogen or protection of ammonia; be heated to 1100-1450 ℃ with 0.5 ℃/minute to 10 ℃/minute heating rate; and be incubated 15 minutes to 4 hours, can on substrate, obtain a large amount of high-purities, highdensity Si 3N 4/ SiO 2Coaxial nano-cable array.
2. according to the described preparation method of claim 1, it is characterized in that: the substrate in the described step (3) is silicon chip, gallium arsenide film, sapphire sheet, silicon nitride single crystal sheet, quartz plate or alumina formwork.
3. according to claim 1 described preparation method, it is characterized in that: deposited thick metallic catalyst Fe, Co, Ni or the Cu film of one deck 2-50nm on the substrate in the described step (3).
4. according to the described preparation method of claim 1, it is characterized in that: carrier gas in the described step (3) and protection gas are higher nitrogen of purity or ammonia, and wherein oxygen partial pressure is 10 -19To 10 -5Between the individual standard atmospheric pressure.
CN2009100894592A 2009-07-21 2009-07-21 Method for preparing high purity, high density and high yield Si3N4/SiO2 coaxial nano-cable array Expired - Fee Related CN101609735B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN2009100894592A CN101609735B (en) 2009-07-21 2009-07-21 Method for preparing high purity, high density and high yield Si3N4/SiO2 coaxial nano-cable array

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN2009100894592A CN101609735B (en) 2009-07-21 2009-07-21 Method for preparing high purity, high density and high yield Si3N4/SiO2 coaxial nano-cable array

Publications (2)

Publication Number Publication Date
CN101609735A true CN101609735A (en) 2009-12-23
CN101609735B CN101609735B (en) 2011-08-31

Family

ID=41483435

Family Applications (1)

Application Number Title Priority Date Filing Date
CN2009100894592A Expired - Fee Related CN101609735B (en) 2009-07-21 2009-07-21 Method for preparing high purity, high density and high yield Si3N4/SiO2 coaxial nano-cable array

Country Status (1)

Country Link
CN (1) CN101609735B (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102477205A (en) * 2010-11-22 2012-05-30 深圳至佳美科技有限公司 Nano modified halogen-free wear resistant cable material and its preparation method
CN102931149A (en) * 2012-11-15 2013-02-13 中国科学院深圳先进技术研究院 Nano-silicon dioxide and nano-silicon nitride composite material and preparation method thereof

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6190634B1 (en) * 1995-06-07 2001-02-20 President And Fellows Of Harvard College Carbide nanomaterials
EP1152827A4 (en) * 1999-01-12 2002-11-06 Hyperion Catalysis Int Carbide and oxycarbide based compositions and nanorods
CN1286123C (en) * 2003-06-27 2006-11-22 西北工业大学 Method for producing noncrystal SiO2 coated SiC coaxial nano cable
CN1312028C (en) * 2005-07-15 2007-04-25 清华大学 Process for synthesizing based si-based one-dimensional nano material
FR2896493B1 (en) * 2006-01-23 2008-02-22 Commissariat Energie Atomique METHOD FOR PRODUCING A SUPPORT FOR THE GROWTH OF LOCALIZED LONG NANOSTRUCTURES

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102477205A (en) * 2010-11-22 2012-05-30 深圳至佳美科技有限公司 Nano modified halogen-free wear resistant cable material and its preparation method
CN102931149A (en) * 2012-11-15 2013-02-13 中国科学院深圳先进技术研究院 Nano-silicon dioxide and nano-silicon nitride composite material and preparation method thereof
CN102931149B (en) * 2012-11-15 2015-06-03 中国科学院深圳先进技术研究院 Nano-silicon dioxide and nano-silicon nitride composite material and preparation method thereof

Also Published As

Publication number Publication date
CN101609735B (en) 2011-08-31

Similar Documents

Publication Publication Date Title
Ivanova et al. Thermoelectric and mechanical properties of the Bi 0.5 Sb 1.5 Te 3 solid solution prepared by melt spinning
CN101434406B (en) Copper germinate nano-wire and preparation thereof
CN101609735B (en) Method for preparing high purity, high density and high yield Si3N4/SiO2 coaxial nano-cable array
Khadher et al. Metal oxide thin films: a mini review
Soomro et al. Growth, structural and optical characterization of ZnO nanotubes on disposable-flexible paper substrates by low-temperature chemical method
Sang et al. Yttrium aluminum garnet nanoparticles synthesized by nitrate decomposition and their low temperature densification behavior
CN100377295C (en) Method for preparing silicon carbide/silicon dioxide co-axial nano cable
CN101603207B (en) Method for preparing network branched silicon nitride single crystal nanostructure with high purity and high yield
Gundiah et al. Carbon-assisted synthesis of silicon nanowires
CN1286123C (en) Method for producing noncrystal SiO2 coated SiC coaxial nano cable
KR101311030B1 (en) Hybrid ink for CZTS film
CN110498448B (en) Layered FeAs, preparation method thereof and FeAs nanosheet stripped therefrom
CN115894042B (en) Ultrahigh-hardness high-entropy metal boride ceramic and low-temperature pressureless method thereof
Maria et al. Zn-dust derived ultrafine grained ZnO non-linear ceramic resistors via in-situ thermal oxidation of cermet reactant mixture
Ye et al. Microstructure and thermal stability of amorphous SiBCNAl powders fabricated by mechanical alloying
Mao et al. Coprecipitation-based micro-reactor process to synthesize soft-agglomerated ultrafine BiPbSrCaCuO powder with low carbon content
Ahlawat Preparation and effect of thermal treatment on Gd 2 O 3: SiO 2 nanocomposite
Gaultois et al. Single-step preparation and consolidation of reduced early-transition-metal oxide/metal n-type thermoelectric composites
Al-Khafaji et al. Effect of catalysts on BN NanoParticles production
CN101550600B (en) A method to prepare a high-purity high-density monocrystalline silicon nitride nano array
CN103787407B (en) Reaction ball milling legal system is for nano TiC N/Al 2o 3the method of composite powder
CN113213438A (en) Boron nitride nanotubes and method for producing the same
Tang et al. Preparation of silicon nanowires by hydrothermal deposition on silicon substrates
CN101531374B (en) Method for producing boron nanowire
Yin et al. Novel route to cubic boron nitride dendritic nanostructures under electron beam irradiation

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C14 Grant of patent or utility model
GR01 Patent grant
C17 Cessation of patent right
CF01 Termination of patent right due to non-payment of annual fee

Granted publication date: 20110831

Termination date: 20120721